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  1. 1

    GLP planning, recording, and archiving /

    Published 2013
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    Series
    Electronic Video
  2. 2

    Performing test systems and test items

    Published 2013
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    Series
    Electronic Video
  3. 3

    In vitro studies and short term studies

    Published 2013
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    Series
    Electronic Video
  4. 4

    History and rationale for the development of an international evaluation programme

    Published 2012
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    Series
    Electronic Video
  5. 5

    Quality assurance

    Published 2012
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    Series
    Electronic Video
  6. 6

    Scope and application

    Published 2012
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    Series
    Electronic Video
  7. 7

    Compliance monitoring systems and their organisation around the world

    Published 2012
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    Series
    Electronic Video
  8. 8

    Reporting of study results

    Published 2012
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    Series
    Electronic Video
  9. 9

    Multi-site studies and field studies

    Published 2012
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    Series
    Electronic Video
  10. 10
  11. 11

    Participation of non-OECD economies in the MAD system

    Published 2012
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    Series
    Electronic Video
  12. 12
  13. 13

    Regulatory requirements in Japan and its compliance monitoring programmes

    Published 2012
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    Series
    Electronic Video
  14. 14

    Why OECD GLP and not ISO / IEC 17025?

    Published 2012
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    Series
    Electronic Video
  15. 15

    GLP in the European Union

    Published 2012
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    Series
    Electronic Video
  16. 16

    Performing, Standard Operating Procedures

    Published 2012
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    Series
    Electronic Video
  17. 17

    Principles of GLP

    Published 2012
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    Series
    Electronic Video
  18. 18

    Inspection procedures

    Published 2012
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    Series
    Electronic Video
  19. 19

    Monitoring GLP compliance history and OECD framework /

    Published 2012
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    Series
    Electronic Video
  20. 20

    Good Laboratory Practice roles and responsibilities /

    Published 2012
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    Series
    Electronic Video